Factors Explaining Interpersonal Variation in Plasma Enterolactone Concentrations in Humans

Lignans are diphenolic plant compounds with potential health modulating properties that are absorbed to the circulation and metabolized to the enterolignans enterodiol (END) and enterolactone (ENL) by gut microbiota. Epidemiological studies have inconsistently shown that a high lignan intake and circulating ENL are associated with reduced risk of breast‐, prostate‐, and colorectal cancer as well as cardiovascular disease and total and cause‐specific mortality. Inconsistencies can be due to interpersonal variation of ENL formation or responses. The aim of this review is to identify and evaluate the impact of factors influencing variability in plasma concentrations of the main enterolignan, ENL. The main determinants of plasma ENL concentrations are intake of lignan and lignan‐rich foods, composition and activity of intestinal microflora, antimicrobial use, nutrient intake, BMI, smoking, sex, and age. Composition and activity of the intestinal microbiota appear to be the most critical factor governing interpersonal variability in plasma ENL concentration followed by the use of antibiotics. Future studies with combined data from gut microbiota and metabolomics with food intake and life style data can be used to estimate the relative contribution of the different factors to ENL concentration in quantitative terms.     

基于可编程模拟器件ispPAC10低频声波声检测电路设计

提出了基于在线可编程模拟器件ispPAC10差动放大及低通滤波电路来完成低频声波信号的采集方法.该方法可有效地降低检测电路的噪声干扰,提高输出信号的信噪比.     

A Capillary Tube Viscometer Designed for Measurements of Hydrogen Gas Viscosity at High Pressure and High Temperature

A capillary tube viscometer was developed to measure the dynamic viscosity of gases for high pressure and high temperature. The apparatus is simple and designed for safe-handling operation. The gas was supplied to the capillary tube from a high-pressure reservoir tank through a pressure regulator unit to maintain a steady state flow. The measurements of a pressure drop across the capillary tube with high accuracy under extreme conditions are the main challenge for this method. A differential pressure sensor for high pressures up to 100 MPa is not available commercially. Therefore, a pair of accurate absolute pressure transducers was used as a differential pressure sensor. Then the pressure drop was calculated by subtracting the outlet pressure from the inlet one with a resolution of 100 Pa at 100 MPa. The accuracy of the present measurement system is confirmed by measuring the viscosity of nitrogen as a reference gas. The apparatus provided viscosities of nitrogen from ambient temperature to 500 K and hydrogen from ambient temperature to 400 K and for pressures up to 100 MPa with a maximum deviation of 2.2 % compared with a correlation developed by the present authors and with REFPROP (NIST).     

Properties of α-, γ-, and δ-tocopherol in purified fish oil triacylglycerols

The effect of α-tocopherol (αTOH) (50–2000 ppm), γ-tocopherol (γTOH) (100–2000 ppm), and δ-tocopherol (δTOH) (100–2000 ppm) on the formation and decomposition of hydroperoxides in purified fish oil triacylglycerols (TAG) was studied. The tests were conducted at 30°C in the dark. Purified fish oil TAG oxidized very rapidly with no apparent induction period. The relative ability of the tocopherols to retard the formation of hydroperoxides decreased in the order αTOH> γTOH>δTOH at a low level of addition (100 ppm), but a reverse order of activity was found when the initial tocopherol concentration was 1000 ppm. This dependence of relative antioxidant activity on tocopherol concentration was caused by the existence of concentrations for maximal antioxidant activity for αTOH and for γTOH. An inversion of activity, on the basis of hydroperoxide formation, was observed for αTOH at 100 ppm and for γTOH at 500 ppm, whereas the antioxidant activity of δTOH increased with level of addition up to 1500–2000 ppm. None of the tocopherols displayed any prooxidant activity. All three tocopherols strongly retarded the formation of volatile secondary oxidation products in a concentration-dependent manner. At concentrations above about 250 ppm there appeared to be a linear relationship between rate of consumption of αTOH and initial αTOH concentration, in accordance with the linear relationship observed between the initial rate of formation of hydroperoxides and the initial αTOH concentration. The rate of consumption of γTOH also increased with initial concentration, but to a lesser extent than for αTOH. At high levels of addition the rate of consumption of δTOH was independent of initial concentration, appearing to reflect the greater stability of this tocopherol homolog and participation in reactions with lipid peroxyl radicals only. Presented in part at the AOCS annual meeting in San Diego, California, April 2000.     

Gamma-Radiolytic Stability of Solvents Containing C5-BPP (2,6-Bis(5-(2,2-dimethylpropyl)-1H-pyrazol-3-yl)pyridine) for Actinide(III)/Lanthanide(III) Separation

The stability of solvents containing the C5-BPP (2,6-Bis(5-(2,2-dimethylpropyl)-1H-pyrazol-3-yl)pyridine) extractant against gamma-irradiation up to 330 kGy adsorbed dose was evaluated using HPLC mass spectrometric and solvent extraction methods. The main radiolysis products were identified using high-resolution mass spectrometry. Quantitative analysis of the residual C5-BPP concentration in irradiated samples was accomplished by a specifically developed MRM (Multiple Reaction Monitoring) method. A mixture of C5-BPP with 2-bromohexanoic acid in kerosene and 1-octanol, which had been used in an actinide(III)/lanthanide(III) separation process demonstration test, was also studied for its radiolytic stability and a remarkable protective effect of the presence of nitric acid during irradiation was found.     

Holistic methodological framework for assessing the benefits of delivering industrial excess heat to a district heating network

In Sweden, over 50% of building heating requirements are covered by district heating. Approximately 8% of the heat supply to district heating systems comes from excess heat from industrial processes. Many studies indicate that there is a potential to substantially increase this share, and policies promoting energy efficiency and greenhouse gas emissions reduction provide incentives to do this. Quantifying the medium and long-term economic and carbon footprint benefits of such investments is difficult because the background energy system against which new investments should be assessed is also expected to undergo significant change as a result of the aforementioned policies. Furthermore, in many cases, the district heating system has already invested or is planning to invest in non-fossil heat sources such as biomass-fueled boilers or CHP units. This paper proposes a holistic methodological framework based on energy market scenarios for assessing the long-term carbon footprint and economic benefits of recovering excess heat from industrial processes for use in district heating systems. In many studies of industrial excess heat, it is assumed that all emissions from the process plant are allocated to the main products, and none to the excess heat. The proposed methodology makes a distinction between unavoidable excess heat and excess heat that could be avoided by increased heat recovery at the plant site, in which case it is assumed that a fraction of the plant emissions should be allocated to the exported heat. The methodology is illustrated through a case study of a chemical complex located approximately 50 km from the city of Gothenburg on the West coast of Sweden, from which substantial amounts of excess heat could be recovered and delivered to heat to the city's district heating network which aims to be completely fossil-free by 2030.     

Towards Molecular Understanding of the Functional Role of UbiJ-UbiK2 Complex in Ubiquinone Biosynthesis by Multiscale Molecular Modelling Studies

Ubiquinone (UQ) is a polyisoprenoid lipid found in the membranes of bacteria and eukaryotes. UQ has important roles, notably in respiratory metabolisms which sustain cellular bioenergetics. Most steps of UQ biosynthesis take place in the cytosol of E. coli within a multiprotein complex called the Ubi metabolon, that contains five enzymes and two accessory proteins, UbiJ and UbiK. The SCP2 domain of UbiJ was proposed to bind the hydrophobic polyisoprenoid tail of UQ biosynthetic intermediates in the Ubi metabolon. How the newly synthesised UQ might be released in the membrane is currently unknown. In this paper, we focused on better understanding the role of the UbiJ-UbiK₂ heterotrimer forming part of the metabolon. Given the difficulties to gain functional insights using biophysical techniques, we applied a multiscale molecular modelling approach to study the UbiJ-UbiK₂ heterotrimer. Our data show that UbiJ-UbiK₂ interacts closely with the membrane and suggests possible pathways to enable the release of UQ into the membrane. This study highlights the UbiJ-UbiK₂ complex as the likely interface between the membrane and the enzymes of the Ubi metabolon and supports that the heterotrimer is key to the biosynthesis of UQ₈ and its release into the membrane of E. coli.     

Mediators in action: Organizing sociotechnical system change

To extend and deepen the roles of mediators in relation to sociotechnical change, this article first suggested an analytical approach which thereafter was used for analysing two cases illustrating two Swedish mediating organizations in different sectors at different time periods: the half state-/half industry funded Research Institute for Water and Air Protection, IVL, in the 1960s and 70s; and the Swedish Urban Network Association, SUNA, in the early years of the 21st century. We found that the associated sociotechnical systems changed through the actions of mediators and their organization of time-spatial specific settings. The mediator concept contributed to our understanding of these changes through a number of visible processes of translating rather than transferring specific knowledge, by functioning as a single entrance to knowledge, by supporting the selection processes, and sometimes by bridging knowledge in unforeseen ways. Overall, the mediating actors took on roles to promote the system and encouraged actors within the system to connect and develop both the system as such.     

Falsely high ionized magnesium results by an ion-selective electrode method in severe hypomagnesemia

Changes in serum total and ionized magnesium (Mg and Mg2+) and calcium (Ca and Ca2+) were monitored in three patients who transiently developed severe (total Mg < 0.50 mmol/l) to profound hypomagnesemia (total Mg < 0.35 mmol/l) due to cisplatin or interleukin-2 therapies. Mg2+ and Ca2+ were measured with the Nova ion-selective electrodes at 37 degrees C and all results were normalized to pH 7.40. Independent of the etiology, the Mg2+ fraction (Mg2+/total Mg) increased as the concentration of the serum total Mg decreased in all three patients. When the total Mg was around or below 0.35 mmol/l the Mg2+ approached or exceeded total Mg, suggesting an error in the measurement of Mg2+. The findings were extended by including a group of 31 additional patients whose serum total Mg, Mg2+, total Ca, and Ca2+ concentrations varied from abnormally low to above normal. The serum total and ionized concentrations strongly correlated for both Mg (r2 = 0.88) and Ca (r2 = 0.92). The Mg2+ fraction rapidly increased with a fall in the total Mg concentration (r2 = 0.76) and total Mg/total Ca ratio (r2 = 0.71). In fact, with decreasing total Mg concentrations or total Mg/total Ca ratios, the Mg2+ fraction progressively increased to 93-128% of the total, confirming an error in the Mg2+ determinations. The Ca2+ fraction showed a slight and insignificant decrease with falling total Ca concentrations and total Mg/total Ca ratios. The Mg2+ concentration was directly related (r2 = 0.62), whereas the Ca2+ concentration showed a complex relationship to the total Mg/total Ca ratio. Whether this latter relationship represents a technical artifact or a true biological phenomenon requires further study. The apparent overestimation of Mg2+ at very low total Mg concentrations, and in the presence of a very low total Mg/total Ca ratio, could be due to improper chemometric correction of the Ca effect on the Mg electrode, non-linearity, and inadequate calibration. Whatever the mechanism, the failure of this method to correctly measure very low serum Mg2+ concentrations in the sera of patients with severe hypomagnesemia, or likely in any patient with an unusually low total Mg/total Ca ratio, erodes its diagnostic usefulness.